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Dorit Lev

Showing results (41-50 of 176) with videos related to

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Journal of Child Neurology|February 3, 2011
Prenatal brain disruption in molybdenum cofactor deficiencyNirit Carmi-Nawi, Gustavo Malinger, Hanna Mandel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 8, 2007
Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?Dorit Lev, Marina Michelson-Kerman, Chana Vinkler, et al.
Clinical Genetics|February 14, 2024
Novel phenotype associated with homozygous likely pathogenic variant in the POP1 geneMarina Michelson, Keren Yosovich, Sarit Bahar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 9, 2006
A benign congenital myopathy in an inbred Samaritan familyDorit Lev, Menachem Sadeh, Nathan Watemberg, et al.
Frontiers in Molecular Neuroscience|October 16, 2018
Photoreceptor Guanylate Cyclase (<i>GUCY2D</i>) Mutations Cause Retinal Dystrophies by Severe Malfunction of Ca<sup>2+</sup>-Dependent Cyclic GMP SynthesisHanna Wimberg, Dorit Lev, Keren Yosovich, et al.
Frontiers in Neuroscience|March 27, 2024
Small size, big problems: insights and difficulties in prenatal diagnosis of fetal microcephalyLeila Haddad, Efrat Hadi, Zvi Leibovitz, et al.
Journal of Child Neurology|February 26, 2009
Developmental outcome of children with enlargement of the cisterna magna identified in uteroRaheli Dror, Gustavo Malinger, Liat Ben-Sira, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 18, 2015
Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1ALubov Blumkin, Esther Leshinsky-Silver, Marina Michelson, et al.
Journal of Neurology|May 29, 2012
A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndromeLubov Blumkin, Sara Kivity, Dorit Lev, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 15, 2010
Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the motherMarina Michelson, Avi Eden, Chana Vinkler, et al.
Pageof 18

Showing results (41-50 of 176) with videos related to

Sort By:
Pageof 18
Journal of Child Neurology|February 3, 2011
Prenatal brain disruption in molybdenum cofactor deficiencyNirit Carmi-Nawi, Gustavo Malinger, Hanna Mandel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 8, 2007
Infantile onset progressive cerebellar atrophy and anterior horn cell degeneration--a late onset variant of PCH-1?Dorit Lev, Marina Michelson-Kerman, Chana Vinkler, et al.
Clinical Genetics|February 14, 2024
Novel phenotype associated with homozygous likely pathogenic variant in the POP1 geneMarina Michelson, Keren Yosovich, Sarit Bahar, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 9, 2006
A benign congenital myopathy in an inbred Samaritan familyDorit Lev, Menachem Sadeh, Nathan Watemberg, et al.
Frontiers in Molecular Neuroscience|October 16, 2018
Photoreceptor Guanylate Cyclase (<i>GUCY2D</i>) Mutations Cause Retinal Dystrophies by Severe Malfunction of Ca<sup>2+</sup>-Dependent Cyclic GMP SynthesisHanna Wimberg, Dorit Lev, Keren Yosovich, et al.
Frontiers in Neuroscience|March 27, 2024
Small size, big problems: insights and difficulties in prenatal diagnosis of fetal microcephalyLeila Haddad, Efrat Hadi, Zvi Leibovitz, et al.
Journal of Child Neurology|February 26, 2009
Developmental outcome of children with enlargement of the cisterna magna identified in uteroRaheli Dror, Gustavo Malinger, Liat Ben-Sira, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 18, 2015
Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1ALubov Blumkin, Esther Leshinsky-Silver, Marina Michelson, et al.
Journal of Neurology|May 29, 2012
A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndromeLubov Blumkin, Sara Kivity, Dorit Lev, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 15, 2010
Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the motherMarina Michelson, Avi Eden, Chana Vinkler, et al.
Pageof 18